P
US8790653B2ExpiredUtilityPatentIndex 39

Peptide inhibitors for mediating stress responses

Assignee: HERKEL JOHANNESPriority: Aug 23, 2004Filed: Nov 1, 2011Granted: Jul 29, 2014
Est. expiryAug 23, 2024(expired)· nominal 20-yr term from priority
Inventors:HERKEL JOHANNESCOHEN IRUN RROTTER VARDALOHSE ANSGAR WEREZ NETAMIMRAN AVISHAIKAM NA AMAN
A61P 39/00A61P 37/00A61P 37/06A61P 7/04A61P 9/10A61P 3/10A61P 7/06A61P 43/00A61P 5/16A61P 35/00A61P 25/28A61P 25/16A61P 27/02A61P 25/00A61P 29/00A61P 31/04A61P 27/06A61P 25/08A61P 19/04A61P 13/12A61P 17/06A61P 19/02A61P 19/00A61P 17/00A61P 11/16A61P 21/04A61P 1/04A61P 17/16A61P 11/00A61P 1/16A61P 19/10A61P 15/08A61P 1/00A61K 39/0005C07K 7/08C07K 14/435A61K 38/00A61K 39/0008C07K 7/06
39
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Claims

Abstract

The present invention relates to peptides capable of inhibiting cellular and immune stress responses in a eukaryotic cell. The invention provides compositions and methods for the treatment of human degenerative diseases and inflammation, utilizing these peptides.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method for treating amyotrophic lateral sclerosis (ALS) in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a peptide comprising an epitope immunoreactive with an anti-idiotypic antibody directed against an anti-p53 antibody, wherein the anti-p53 antibody is immunoreactive with at least a part of the regulatory domain of the C-terminus of p53, and wherein the peptide exhibits at least one activity selected from anti-apoptotic activity and anti-inflammatory activity wherein the length of the peptide is 7 to 25 amino acids and has the amino acid sequence as set forth in SEQ ID NO: 1. 
     
     
       2. The method of  claim 1 , wherein the anti-p53 antibody is PAb-421. 
     
     
       3. The method of  claim 1 , wherein the amino acid sequence of said peptide is as set forth in SEQ ID NO: 1. 
     
     
       4. The method of  claim 1 , wherein the peptide is administered to the subject by a route selected from oral, topical, transdermal and parenteral.

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